Citalopram for Agitation in Alzheimer's Disease

NCT00898807 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 186

Last updated 2014-06-27

Study results available
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Summary

The purpose of this study is to evaluate the safety and efficacy of citalopram for agitation in Alzheimer's dementia.

Conditions

Interventions

DRUG

citalopram

target dose 30mg daily for 9 weeks

DRUG

placebo

daily for 9 weeks

Sponsors & Collaborators

  • National Institute on Aging (NIA)

    collaborator NIH
  • National Institute of Mental Health (NIMH)

    collaborator NIH
  • JHSPH Center for Clinical Trials

    lead OTHER

Principal Investigators

  • Constantine Lyketsos, MD, MHS · Johns Hopkins University

  • Lon Schneider, MD · University of Southern California Keck School of Medicine Memory and Aging Center

  • Bruce Pollock, MD · Centre for Addiction and Mental Health

  • Jacobo Mintzer, MD · Medical University of South Carolina Alzheimer's Research and Clinical Programs

  • David Shade, Esq · Johns Hopkins University

  • Davengere Devanand, MD · Columbia University

  • Paul Rosenberg, MD · Johns Hopkins University

  • Daniel Weintraub, MD · University of Pennsylvania

  • Anton Porsteinsson, MD · University of Rochester

  • Jerome Yesavage, MD · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00898807 on ClinicalTrials.gov